|Publication number||US3685345 A|
|Publication date||Aug 22, 1972|
|Filing date||May 15, 1970|
|Priority date||May 15, 1970|
|Also published as||CA929087A, CA929087A1|
|Publication number||US 3685345 A, US 3685345A, US-A-3685345, US3685345 A, US3685345A|
|Inventors||Wise Harold L|
|Original Assignee||Wise Harold L|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (5), Referenced by (25), Classifications (18)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 5 Wise EQUILIBRATED SOIL-GAS SAMPLING Inventor: Harold L. Wise, 4522 Hummingbird, Houston, Tex. 77035 Filed: May 15, 1970 Appl. No.: 37,607
US. Cl ..73/19, 73/152, 73/61 R,
23/230 EP, 73/421.5 R Int. Cl. ..G0ln l/00, GOln 31/00 Field of Search...73/19, 23, 155, 152, 61, 421.5;
References Cited UNITED STATES PATENTS 7/1934 Quereau ..73/28 X 5/1958 Clift ..73/421 [151 3,685,345 51 Aug. 22, 1972 2,479,787 8/1949 Stevens ..23/23O 2,861,450 11/1958 Rausley ..73/19 2,987,912 6/1961 Jacobson ..73/19 Primary Examiner-Richard C. Queisser Assistant ExaminerC. E. Snee, Ill Attorney-Harold W. Coryell and J. H. McCarthy 1 1 ABSTRACT The sampling of the concentration of a selected fluid in a subterranean earth formation is improved by circulating a fluid into repetitive contacts with the earth formation and measuring the concentration of the selected fluid in the circulating fluid when the concentration is at a level at which its rate of change is low relative to that exhibited in the initial stage of the fluid circulation.
10 Claims, 1 Drawing Figure PATENTEDnuszz m2 INVENTOR.
HAROLD L. WISE ATTORNFY EQUILIBRATED SOIL-GAS SAMPLING BACKGROUND OF THE INVENTION The invention relates to the sampling of soils or other subsurface earth formations. Such a sampling is often used to provide maps or surveys of the concentration with location of at least one selected fluid. Such maps are indicative of compositions and/or events within the sampled or underlying subterranean earth formations.
Numerous methods and devices have been proposed for sampling the concentration of a fluid, such as a hydrocarbon, in a subterranean earth formation. Such operations are made difficult by the tendency for the concentrations of such fluids to be very small; generally less than one part per million. At such relatively low concentrations the previously employed sampling procedures have tended to provide inconclusive results. The concentrations that were measured at times and locations at which the measured values should have been substantially equal have tended to fluctuate by amounts that were large relative to the amounts that were present, have tended to follow changes in the concentrations in the ambient atmosphere, have tended to vary widely from one sample to the next, etc.
Fluids such as hydrocarbons tend to escape from subterranean locations and migrate up through the overlying earth formations. Some of the migrating fluids become adsorbed on the solid components of the earth formations and some become dissolved or entrained in the fluid components. The hydrocarbons associated with both the solid and liquid components of an earth formation can be measured by obtaining and analyzing a core sample; but, it is relatively expensive to collect and analyze such samples. In general, the previously proposed procedures for sampling subsurface earth formations are based on analyses of the fluid encountered by a borehole that is opened into the earth formation. In such procedures, the pressure within the borehole is reduced to one which is less than that within the earth formation, a portion of inflowing fluid is collected, and measurements are made of the hydrocarbon content of that fluid. At depths above the water table the so-collected fluids are usually gaseous and at depths greater than the water table they are usually liquid. 1
A primary object of the present invention is the provision of an economically feasible sampling procedure that is responsive to any natural correlation that may exist between the amounts and types of a selected fluid, such as a hydrocarbon, that are contained in subsurface earth formations that have different horizontal or vertical locations.
In a permeable earth formation the mineral solids are adapted to adsorb varying amounts of hydrocarbons of different compositions or types. The solid components are surrounded by one or more fluids that each have a different degree of miscibility with hydrocarbons of varying types. If the naturally occurring (or connate) fluid in the earth formation is sampled, its hydrocarbon content is a function of the chemical composition and phase of the fluid as well as the type and amount of hydrocarbons that may have migrated into or through that portion of earth formation. If the fluid contents are all that is analyzed, this is apt to provide results that are misleading with respect to the hydrocarbon contents of differently located portions of earth formations. For ex ample, if portions of the same type of permeable earth formation solid materials are located above and below the water table and are traversed by the same upward migration volatile hydrocarbons, the hydrocarbon content of the fluids in the upper location (e.g., gases similar to the ambient atmospheric gas) would be distinctly different from those of the fluid in the lower location (e.g.,' an aqueous solution of one or more salts). In other words, generally similar amounts and types of hydrocarbons may be adsorbed on the earth formation solids in both locations, but distinctly different amounts and types may be dissolved and/or entrained in, for example, a fully miscible gaseous fluid and a substantially immiscible aqueous liquid.
SUMMARY OF THIS INVENTION This invention provides an improved process for measuring the amount of a selected fluid that is present in a subsurface earth formation into which a borehole is opened. In the present process a fluid that contains a known and relatively small amount of the fluid being sampled is circulated i'nto repetitive contacts with the earth formation and the concentration in the circulation fluid of the fluid being sampled is measured at a substantially equilibrium value at which its rate of change is low relative to that exhibited in early stages-of the fluid circulation.
The present invention is particularly useful for measuring the concentration with position of one or more selected fluids that may be indicative of a subterranean deposit or source of such a fluid. It is also useful for monitoring a concentration of a selected fluid with time (or other parameter) in order to detect a presence or an event in the earth formation being sampled or in an underlying earth formation.
DESCRIPTION OF THE DRAWING The FIGURE is a schematic illustration of equipment disposed for sampling an earth formation in accordance with this invention.
DESCRIPTION OF THE INVENTION In the system shown in the drawing, a borehole l is opened into a subsurface earth formation 2 to be sampled with respect to its content of a selected fluid such as ethane. Pump 3 is arranged to circulate fluid through pump inflow and outlet conduits 4 and 5 which are attached, by means of connectors 6 and 7, to borehole conduits 8 and 9. The borehole conduits extend through and are supported by borehole closure plug 10. The connectors 6 and 7 are arranged so that conduits 4 and 5 can be disconnected from the borehole conduits and connected together, by means of detachable conduit (not shown) in order to confine the pump-driven fluid circulation path to a surface location. Multiple port valve 11 is arranged to switch a sample trap loop 12 into and out of the pump-driven fluid circulation path.
Valve 1 l, in the position shown, connects a source of pressurized fluid 13 so that fluid flowing from source 13 displaces fluid from the trap loop 12 into chromatographic column 14, and then into a measuring device 15, and, subsequently, out through an exhaust port, 16.
Flow-controling valve means, such as throttle valve 18 and check valve 19, can advantageously be used when operating the column 14 at a pressure higher than that generated by pump 3. Throttle valve 18 can restrict the rate at which fluid flows from a relatively high pressure at source 13 to atmospheric pressure at exhaust port 16, thus maintaining a selected relatively high pressure within column 14. It also causes trap loop 12 to become filled with gas at about the pressure in column 14. Where the pressure in column 14 is greater than that provided by pump 3 the amount of gas in loop 12 is more than that in the same-sized portion of conduit 5. Repeated switchings of trap loop 12 between the higher and lower pressures tends to dilute the fluid being recirculated within the borehole by removing relatively small amounts and replacing them with larger amounts. Such a dilution is preferably avoided by arranging check valve 19 to allow an outflow through port 20 in response to a pressure above that provided by pump 3.
In a preferred mode of operating the system shown in the drawing, the surface located portion of the circulation path is purged and filled with a substantially hydrocarbon-free gas, such as a clean air. Such an operation preferably includes an interconnection of the pump inflow and outflow conduits 4 and 5 through connectors 6 and 7 and a detachable conduit (not shown) to form a limited circulation pat that is closed, except for the exhaust through check valve 19. This limited circulation path is preferably purged and filled with hydrocarbon-free fluid from a source such as source 13. When the borehole is drilled, plug is inserted promptly to isolate the borehole form atmospheric gases. The portions of the connectors 6 and 7 that are attached to the borehole conduits 8 and 9 are preferably arranged so that they close the ends of those conduits when the conduits are disconnected from the surface located portion of the circulation path.
In operating the invention, the circulation of a hydrocarbon-free gas into repetitive contacts with the earth formation is initiated with the system arranged as shown in the drawing, except that valve 11 is positioned so that trap loop 12 is in the path of the pump-drive circulation into the borehole. During this operation, the fluid within the borehole above the lower ends of the conduits 8 and 9 remains substantially static. The fluid which circulates within the borehole tends to follow the arrows and to selectively contact the portions of earth formation to that are exposed within the region bounded by the broken line 17.
In a shallow borehole, e. g., one having a depth in the order of 5 feet, the fluid pressure within the earth for mation is substantially atmospheric pressure. By selecting conduits 4, 5, 8 and 9 to have substantially equal sizes and effective flow resistances, the pressure of the fluid being circulated within the borehole can be maintained at substantially atmospheric pressure. This causes the exposed earth formations in zone 17 to be repetitively contacted while little or no fluid is being lost into or withdrawn from the portions that are not swept by the fluid circulating within the borehole.
In general, the boreholes used in the present invention can be relatively deep or shallow and can be freshly drilled or pre-existing. Freshly drilled shallow boreholes are preferred. Particularly suitable boreholes are drilled with an augering type of device which requires no circulation of drilling fluid. The augering of a borehole tends to mechanically displace earth formation solids so that a limited amount of fluid is drawn into the lower part of the borehole. The amount drawn in is only that required to replace the material that is removed and it is drawn in from the earth formations adjacent to the lower part of the borehole. The freshly drilled boreholes are preferably promptly plugged or packed-off at least at a depth near the depth at which the sampling is to be conducted. Field tests have demonstrated that even where the atmosphere is polluted with significant and varying amounts of hydrocarbons, consistent and reproducible measurements of hydrocarbon concentrations can be made by: removing solid material from subsurface earth formations to form a borehole while inflowing fluid substantially only from surrounding subsurface earth formations, promptly isolating the portion of the borehole wall which is to be sampled from fluids in the overlying atmosphere, and sampling the hydrocarbon concentration of the so-exposed earth formation by circulating a substantially hydrocarbon-free fluid and measuring its hydrocarbon content as described above.
in relatively deep boreholes, the exposed earth formations may contain a liquid having a significantly high pressure and temperature. In such situations the sample-entraining fluid, i.e., the fluid containing a known and relatively insignificant amount of the fluid whose concentration is being sampled, can be either a gas or a liquid. In either situation the borehole is preferably equipped with conduits, packers, etc., arranged to confine the fluid being circulated so that it makes repeti tive contacts with the earth formations that are exposed along a selected depth interval. Such a circulating fluid is preferably circulated against a back pressure adjusted to provide a downhole pressure substantially equalling the pressure of the fluid within the exposed earth formations. The measurements of the concentration of the selected fluid within the circulating fluid are preferably accompanied by measurements of the pressure and temperature of the circulating fluid.
The fluid that is sampled or surveyed by the present invention can be substantially any gas or liquid. One or more hydrocarbons containing from about one to 10 carbon atoms, carbon dioxide, nitrogen, oxygen, hydrogen sulfide, or the like comprise preferred fluids to be sampled.
The sample-entraining fluid which is circulated into repetitive contacts with the earth formation being sampled can be substantially any pumpable fluid the (a) is at least substantially miscible with the fluid being sampled and (b) is substantially free of the fluid sampled. In general, for sampling the concentration of either an organic or inorganic gas, vapor, air or liquid, that is substantially free of the fluid being sampled is a preferred sample-entraining fluid. In certain locations, the ambient atmospheric air substantially free of contaminants. Such uncontaminated air can be tanked and utilized in the manner illustrated in the drawing and/or can be pressurized by means of the compressor or blower to displace it into the circulating and analyzing system.
The rate and duration of the circulation of sampleentraining fluid can vary over a relative wide range. In a given situation, the sample-entraining fluid should be circulated until the rate of change of the concentration of the fluid being sampled is low relative to its rate of change in the early stages of the fluid circulation. This amounts to sampling a substantially equilibrium concentration. It is the preferred concentration to be measured in accordance with the present invention as that which is representative of the sampled portion of an earth formation. It is a concentration at which the rate at which the selected fluid is being desorbed (or otherwise released from or discharged from the exposed portion of the earth formation) is substantially equal to (or is substantially constant with respect to) the rate at which that fluid is adsorbed on the exposed earth formation. In a given situation the attainment of this substantial equilibrium concentration can be determined by repetitively measuring the concentration during the fluid circulation and noting the circulation time required for the attainment of a relatively low rate of change of concentration. Where the same type of formations are being sampled with the same sample-entraining fluid and the same size of boreholes, circulation equipment, circulation rate, and the like, are used, the making of repetitive measurements can be omitted and a substantially equilibrium concentration can be measured by making each of the measurements at about the same times after the initiations of the circulations.
While the present invention is not limited to any particular mechanism or theory of operation, it appears to selectively sample fluid which is either being desorbed by the contacting of the earth formation with the circulating sample-entraining fluid or is flowing through the contacted portion of the earth formation while it is being contacted by the sample-entraining fluid. After the borehole has been opened, the fluid which was present in the surrounding portions of the earth formation prior to the drilling of the borehole is, in effect, held back and kept out of the path of the circulating sample-entraining fluid. Since the sample-entraining fluid is circulated at a pressure equalling the formation fluid pressure, its flow tends to be confined to a region near the inflow and discharge openings of the conduits to which it is circulated. The present invention thus minimizes variations in the measured concentrations that might be due to variations in the type of fluid that was initially present in different portions of the earth formation.
The consistency of the attainment of substantially equilibrium concentrations and the reproducibility of the present sampling procedure have been demonstrated in repetitive measurements in earth formations in which the concentrations of the hydrocarbons should be the same. The boreholes were drilled to a depth of about 5 feet with a bronze auger having a diameter of about 4 inches. The measurements were made with sampling equipment of the type shown in the drawing. The sample-entraining fluid was atmospheric air that was preprocessed to render it substantially free of hydrocarbons. In a region and a time in which the concentrations of the measured hydrocarbon in the ambient atmosphere ranged from 80 to 100 units, measurements in a series of boreholes in equivalent locations settled to relatively slow and constant rates of change within 1 to 2 minutes after the starts of the circulation of the sample-entraining fluid. Within a period of 30 minutes the measured concentrations remained consistently with a range of from 1,400 to 1,500 units in boreholes of relatively high hydrocarbon concentration and within a range of from 10 to 20 units in boreholes of relatively low hydrocarbon concentration. Note that neither range seems likely to have involved significant contamination by the ambient atmosphere, in which the hydrocarbon concentration was distinctly different.
Such measurements have confirmed the conclusion that (1) consistent and representative substantially equilibrium concentrations can be measured at equal times after the starts of the circulations of the sampleentraining fluid (2) atmospheric contamination can be avoided (3) the measurements are reproducible in the range of less than one part per million concentration (4) in boreholes in which the amounts of hydrocarbons are high, within such a range, the concentrations tend to be relatively slowly increasing with time and (5) in boreholes in which the concentrations are low within such a range the concentrations tend to be relatively slowly decreasing with time. The location of boreholes in which the concentration of hydrocarbons increased with time seem to be in the direct paths of fluids that are migrating through the earth formations being sampled. Such an increase is also observable in the concentrations of other gases such as CO N etc., that may be copresent with hydrocarbons in gas reservoirs.
What is claimed is:
1. A geochemical exploration process, which comprises:
opening a borehole into a subsurface earth formation;
installing within said borehole means for conveying fluid to and from selected depths within the borehole; installing a packing or plugging means adjacent to the section of borehole that contains said selected depths to isolate that section by preventing the flow of fluid between the wall of the borehole and the exterior of said means for conveying fluid;
circulating a fluid that contains a known and relatively insignificant concentration of a selected fluid into repetitive contacts with earth formations exposed along the wall of the borehole at said selected depths; and
measuring the concentration of the selected fluid within the circulating fluid when the rate of change of its concentration is slow relative to the rate of change in an initial stage of the fluid concentration.
2. The process of claim 1 in which the pressure of the fluid circulating within said borehole is kept substantially equal to the pressure of the fluid in said exposed earth formations.
3. In a process for measuring the concentration of at least one hydrocarbon in a subsurface earth formation that is exposed along the wall of a borehole, the improvement which comprises:
mechanically isolating a selected depth within said borehole;
circulating fluid having a known and relatively insignificant concentration of the selected hydrocarbon into repetitive contacts with the earth formation that is exposed at said selected depth within the borehole; and
measuring the concentration of the selected hydrocarbon in the circulating fluid when the rate of change of its concentration is slow relative to that exhibited near the start of said fluid circulatron.
4. The process of claim 3 in which the pressure of the circulating fluid is kept substantially equal to the pressure of the fluid within the subsurface earth formation.
5. The process of claim 3 in which the measurements are made in a plurality of boreholes by circulating the same type of fluid into each borehole.
6. The process of claim 3 in which the measurements are made of at least one inorganic component that is copresent with at least one hydrocarbon.
7. The process of claim 3 in which the borehole is formed by mechanically removing solids while inflowing fluid from the adjacent subsurface earth formations without pumping any significant amount of fluid into 5 the borehole from a surface location.
8. The process of claim 7 in which the borehole is formed by an augering out said solids to create a reduced pressure near the bottom of the borehole.
9. The process of claim 3 in which the circulation of fluid is started substantially immediately after the borehole is opened into the earth formation.
10. The process of claim 3 in which the circulated fluid is air that contains less than one part per million of any hydrocarbon.
*zgw UNITED STATES PATENT OFFICE CERTIFICATE OF (ZORRECTION Patent No- 5, 5,3 5 Dated Augist 22, 1972 Inventor(s) Harold L. Wise It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
The patent is assigned to Shell Oil Company New York,
New York, a Corporation of Delaware.
Signed and sealed this 23rd day of January 1973.
ROBERT GOTTSCHALK Commissioner of Patents EDWARD M. FLETCHER,JR. Attesting Officer -9 I TEBzGP g g UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. ,685,3 5 Dated August 22, 1972 Inventor(x) Harold L; Wise It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
' I'he oafcerf; is assigned to Shell Oil Company,
New York, New York, a Corporation of Delaware.
Signed and sealed this 15th day oI May 1973.
EDWARD M.FLETCHER,JR. ROBERT GO'I'TSCI-IALK Attesting Officer Commissioner of Patents
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US1967428 *||Sep 30, 1931||Jul 24, 1934||Leeds & Northrup Co||Fluid sampling system|
|US2479787 *||Dec 23, 1944||Aug 23, 1949||Socony Vacuum Oil Co Inc||Geophysical prospecting method|
|US2836068 *||May 21, 1954||May 27, 1958||Standard Oil Co||Tank sampling apparatus|
|US2861450 *||Aug 8, 1955||Nov 25, 1958||British Aluminum Company Ltd||Determination of the gas content of liquid metals|
|US2987912 *||Jun 1, 1956||Jun 13, 1961||Mine Safety Appliances Co||Method and apparatus for measurement of gas dissolved in a liquid|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3857289 *||Aug 22, 1973||Dec 31, 1974||Shell Oil Co||Soil sampling auger|
|US4090398 *||Jan 3, 1977||May 23, 1978||Exxon Production Research Company||Method for determining fluid saturations in reservoirs|
|US4158957 *||Feb 16, 1978||Jun 26, 1979||Exxon Production Research Company||Method for determining the fluid saturation of an immobile phase in a reservoir|
|US4827775 *||Jul 17, 1987||May 9, 1989||Gilbert Forrester||Apparatus for extracting a sample|
|US5421419 *||Sep 21, 1993||Jun 6, 1995||Simulprobe Technologies, Inc.||Method and apparatus for fluid and soil sampling|
|US5743343 *||Mar 15, 1995||Apr 28, 1998||Simulprobe Technologies, Inc.||Method and apparatus for fluid and soil sampling|
|US5786527 *||Apr 12, 1995||Jul 28, 1998||Tarte; Andre||Method and apparatus for testing soil contamination|
|US5884714 *||May 24, 1995||Mar 23, 1999||Simulprobe Technologies, Inc.||Method and apparatus for fluid and soil sampling|
|US5979569 *||Nov 6, 1995||Nov 9, 1999||Simulprobe Technologies, Inc.||Method and apparatus for environmental sampling|
|US5992213 *||Jul 20, 1998||Nov 30, 1999||Tartre; Andre||Method for testing soil contamination|
|US6000481 *||May 13, 1996||Dec 14, 1999||Simulprobe Technologies, Inc.||Method and apparatus for environmental sampling|
|US6035950 *||Apr 28, 1998||Mar 14, 2000||Simulprobe Technologies, Inc.||Method and apparatus for fluid and soil sampling|
|US6289714||Oct 5, 1999||Sep 18, 2001||TARTRE ANDRé||Method for testing soil contamination, and probe therefor|
|US6499362 *||Dec 3, 2001||Dec 31, 2002||Global Fia, Inc.||In-line filter probe for process analysis|
|US7028562||Feb 6, 2004||Apr 18, 2006||University Of Maryland, Baltimore County||Vacuum membrane extraction system|
|US7520186 *||May 18, 2006||Apr 21, 2009||St. Francis Xavier University||Apparatus and method for measuring soil gases|
|US7666679 *||Feb 23, 2010||Institut Francais Du Petrole||Method and device for analyzing the CO2 contained in a drilling fluid|
|US9297725 *||Jun 29, 2012||Mar 29, 2016||Korea Institute Of Geoscience And Mineral Resources||Apparatus for extracting, analyzing, and storing gas in drilled core on ship|
|US20040154414 *||Feb 6, 2004||Aug 12, 2004||Lacourse William R.||Vacuum membrane extraction system|
|US20040203160 *||Mar 11, 2004||Oct 14, 2004||Benjamin Herzhaft||Method and device for analyzing the CO2 contained in a drilling fluid|
|US20070266800 *||May 18, 2006||Nov 22, 2007||Risk David A||Apparatus and method for measuring soil gases|
|US20130239672 *||Jun 29, 2012||Sep 19, 2013||Korea Institute Of Geoscience And Mineral Resources||Apparatus for extracting, analyzing, and storing gas in drilled core on ship|
|DE3444363A1 *||Dec 5, 1984||Jun 12, 1986||Quantitative Environmental Dec||Device for taking liquid samples|
|EP1457778A1 *||Feb 20, 2004||Sep 15, 2004||Institut Français du Pétrole||Method and device for analysing the CO2 content of a borehole fluid|
|WO1995027911A1 *||Apr 12, 1995||Oct 19, 1995||Societe D'expertise Envirotest Ltee||Method and apparatus for testing soil contamination|
|U.S. Classification||73/19.1, 73/152.55, 73/61.41, 73/864.81, 73/863.21, 436/30, 73/864.33|
|International Classification||E21B49/00, G01N33/24, G01N1/22, G01N1/14|
|Cooperative Classification||E21B49/005, G01N33/241, G01N1/2294, G01N1/14|
|European Classification||G01N33/24A, E21B49/00G, G01N1/14|